EDA polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS7451
Background:
The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene.
Alternative Name:
Ectodermal dysplasia 1, anhidrotic, Ectodermal dysplasia protein, Ectodermal dysplasia, anhidrotic (hypohydrotic), Ectodysplasin A, Ectodysplasin A, membrane form, Ectodysplasin A, secreted form, ECTODYSPLASIN A1 ISOFORM, ECTODYSPLASIN A2 ISOFORM, ECTODYSPLASIN, Ectodysplasin-A, ED1 A1, ED1 A2, ED1, ED1 GENE, Eda A1, Eda A2, eda, EDA protein, EDA protein homolog, EDA_HUMAN, EDA1, EDA1 GENE, EDA2, HED, ODT1, Oligodontia 1, secreted form, STHAGX1, Ta, Tabby, Tabby protein, X linked anhidroitic ectodermal dysplasia protein, XHED, XLHED,
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: EDA polyclonal antibody detects endogenous levels of EDA protein.
Immunogen:
Recombinant full length Human EDA.
MW: ~49 kDa
Swis Prot.: Q92838
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene.
Alternative Name:
Ectodermal dysplasia 1, anhidrotic, Ectodermal dysplasia protein, Ectodermal dysplasia, anhidrotic (hypohydrotic), Ectodysplasin A, Ectodysplasin A, membrane form, Ectodysplasin A, secreted form, ECTODYSPLASIN A1 ISOFORM, ECTODYSPLASIN A2 ISOFORM, ECTODYSPLASIN, Ectodysplasin-A, ED1 A1, ED1 A2, ED1, ED1 GENE, Eda A1, Eda A2, eda, EDA protein, EDA protein homolog, EDA_HUMAN, EDA1, EDA1 GENE, EDA2, HED, ODT1, Oligodontia 1, secreted form, STHAGX1, Ta, Tabby, Tabby protein, X linked anhidroitic ectodermal dysplasia protein, XHED, XLHED,
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: EDA polyclonal antibody detects endogenous levels of EDA protein.
Immunogen:
Recombinant full length Human EDA.
MW: ~49 kDa
Swis Prot.: Q92838
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
| Is Featured? | No |
|---|
Write Your Own Review